Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled by Encore Medical, LP Due to Due to packaging discrepancy with the incorrect tibial...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Encore Medical, LP directly.
Affected Products
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Software Version: NA Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femoral heads and all hip stems Component: NA
Quantity: 20 units
Why Was This Recalled?
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
Where Was This Sold?
This product was distributed to 14 states: AL, CA, FL, IN, LA, MD, MI, NY, NC, TN, TX, UT, VT, VA
About Encore Medical, LP
Encore Medical, LP has 54 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report